rs121918090, TTR

N. diseases: 8
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
CUI: C2751492
Disease: AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
68 0.790 0.240 18 31593026 missense variant G/C snv 0.810 1.000 26 1986 2016
Adenomatous Polyposis Coli
CUI: C0032580
Disease: Adenomatous Polyposis Coli
237 0.790 0.240 18 31593026 missense variant G/C snv 0.010 1.000 1 2002 2002
Amyloid Neuropathies
CUI: C0206247
Disease: Amyloid Neuropathies
3 0.790 0.240 18 31593026 missense variant G/C snv 0.010 1.000 1 2013 2013
Amyloidosis, Familial
CUI: C0740340
Disease: Amyloidosis, Familial
12 0.790 0.240 18 31593026 missense variant G/C snv 0.010 1.000 1 2013 2013
Cardiomyopathies
CUI: C0878544
Disease: Cardiomyopathies
294 0.790 0.240 18 31593026 missense variant G/C snv 0.010 1.000 1 2002 2002
Congestive heart failure
CUI: C0018802
Disease: Congestive heart failure
165 0.790 0.240 18 31593026 missense variant G/C snv 0.010 1.000 1 2000 2000
Heart failure
CUI: C0018801
Disease: Heart failure
201 0.790 0.240 18 31593026 missense variant G/C snv 0.010 1.000 1 2000 2000
Polyneuropathy
CUI: C0152025
Disease: Polyneuropathy
32 0.790 0.240 18 31593026 missense variant G/C snv 0.010 1.000 1 2000 2000